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Title: | Engineered osteoclasts resorb necrotic alveolar bone in anti-RANKL antibody-treated mice |
Authors: | Worakanya Buranaphatthana Apichai Yavirach Elizabeth M. Leaf Marta Scatena Hai Zhang Jonathan Y. An Cecilia M. Giachelli |
Authors: | Worakanya Buranaphatthana Apichai Yavirach Elizabeth M. Leaf Marta Scatena Hai Zhang Jonathan Y. An Cecilia M. Giachelli |
Keywords: | Biochemistry, Genetics and Molecular Biology;Medicine |
Issue Date: | 1-Dec-2021 |
Abstract: | Medication-related osteonecrosis of the jaw (MRONJ) is a serious side effect of antiresorptive medications such as denosumab (humanized anti-RANKL antibody), yet its pathophysiology remains elusive. It has been posited that inhibition of osteoclastic bone resorption leads to the pathological sequelae of dead bone accumulation, impaired new bone formation, and poor wound healing in MRONJ, but this hypothesis has not been definitively tested. We previously engineered myeloid precursors with a conditional receptor activator of nuclear factor kappa-Β intracellular domain (iRANK cells), which differentiate into osteoclasts in response to a chemical inducer of dimerization (CID) independently of RANKL. In this study, we showed that CID-treated iRANK cells differentiated into osteoclasts and robustly resorbed mineralized surfaces even in the presence of anti-RANKL antibody in vitro. We then developed a tooth extraction-triggered MRONJ model in nude mice using anti-RANKL antibody to deplete osteoclasts. This model was used to determine whether reconstitution of engineered osteoclasts within sockets could prevent specific pathological features of MRONJ. Locally delivered iRANK cells successfully differentiated into multinucleated osteoclasts in response to CID treatment in vivo as measured by green fluorescent protein (GFP), tartrate-resistant acid phosphatase (TRAP), carbonic anhydrase II, matrix metallopeptidase 9 (MMP-9), and cathepsin K staining. Sockets treated with iRANK cells + CID had significantly more osteoclasts and less necrotic bone than those receiving iRANK cells alone. These data support the hypothesis that osteoclast deficiency leads to accumulation of necrotic bone in MRONJ. |
URI: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85113228183&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/75501 |
ISSN: | 87563282 |
Appears in Collections: | CMUL: Journal Articles |
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